A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496766



Internal ID20869969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87244288..87248370hg38UCSC Ensembl
chr16:87277894..87281976hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg384083
hg194083
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18033607
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496766
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer